HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627026Generated: November 2, 2026
Sodium hydride → HCID 117871199, compound
https://huagongshe.com/reaction/627026
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-carbobenzyloxyalanine | HCID 736104 | — |
| Reactant | 2-(Methylsulfonyl)ethyl methanesulfonate | HCID 18464597 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117871199 | HCID 117871199 | 41.2% |
Reaction Steps
In a 100 mL round-bottomed flask, (S)-2-(benzyloxycarbonylamino)propanoic acid (331 mg, 1.48 mmol, Eq: 1.00) was combined with THF (9 mL) to give a colorless solution. Sodium hydride (131 mg, 3.26 mmol, Eq: 2.2) was added. The reaction was stirred at rt for 30 min, then 2-(methylsulfonyl)ethyl methanesulfonate (300 mg, 1.48 mmol, Eq: 1.00) was added and the reaction was stirred at rt overnight. The reaction was quenched with saturated aqueous NH4Cl and extracted with EtOAc. The combined organic layers were washed with water and brine then dried over Na2SO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 40 g, 10% to 60% EtOAc in hexanes) to give (S)-2-[benzyloxycarbonyl-(2-methanesulfonyl-ethyl)-amino]-propionic acid (201 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309248B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-38185ec196f44befa7d7885b6a987231 |
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| Source note | uspto-grants-2016_04 |
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